Siniatchkin Michael, van Baalen Andreas, Jacobs Julia, Moeller Friederike, Moehring Jan, Boor Rainer, Wolff Stephan, Jansen Olav, Stephani Ulrich
Department of Neuropediatrics, Christian-Albrechts-University of Kiel, Kiel, Germany.
Epilepsia. 2007 Dec;48(12):2312-21. doi: 10.1111/j.1528-1167.2007.01195.x. Epub 2007 Jul 21.
West syndrome is a severe epileptic encephalopathy of infancy characterized by a poor developmental outcome and hypsarrhythmia. The pathogenesis of hypsarrhythmia is insufficiently understood.
We investigated eight patients with infantile spasms and hypsarrhythmia (group I) and 8 children with complex partial seizures (group II) using simultaneous recordings of electroencephalogram (EEG) and functional MRI. Hemodynamic responses to epileptiform discharges and slow wave activity (EEG delta power) were analyzed separately.
In group I (mean age, 7.82 +/- 2.87 months), interictal spikes within the hypsarrhythmia were associated with positive blood oxygenation level-dependent (BOLD) changes in the cerebral cortex (especially occipital areas). This was comparable with cortical positive BOLD responses in group II (mean age, 20.75 +/- 12.52 months). Slow wave activity in group I correlated significantly with BOLD signal in voxels, which were localized in brainstem, thalamus, as well as different cortical areas. There was no association between BOLD effect and EEG delta power in group II. Moreover, as revealed by group analysis, group I differed from group II according to correlations between BOLD signal and slow wave activity in putamen and brainstem.
This study demonstrates that multifocal interictal spikes and high-amplitude slow wave activity within the hypsarrhythmia are associated with the activation of different neuronal networks. Although spikes caused a cortical activation pattern similar to that in focal epilepsies, slow wave activity produced a hypsarrhythmia-specific activation in cortex and subcortical structures such as brainstem, thalamus, and putamen.
韦斯特综合征是一种婴儿期严重的癫痫性脑病,其特征为发育不良和高峰失律。高峰失律的发病机制尚未完全明确。
我们对8例患有婴儿痉挛症和高峰失律的患者(第一组)以及8例复杂部分性发作的儿童(第二组)进行了脑电图(EEG)和功能磁共振成像(fMRI)同步记录。分别分析了癫痫样放电和慢波活动(EEGδ波功率)的血流动力学反应。
在第一组(平均年龄7.82±2.87个月)中,高峰失律期间的发作间期棘波与大脑皮层(尤其是枕叶区域)的正性血氧水平依赖(BOLD)变化相关。这与第二组(平均年龄20.75±12.52个月)的皮层正性BOLD反应相当。第一组的慢波活动与位于脑干、丘脑以及不同皮层区域的体素中的BOLD信号显著相关。第二组中BOLD效应与EEGδ波功率之间无关联。此外,通过组分析发现,根据壳核和脑干中BOLD信号与慢波活动之间的相关性,第一组与第二组不同。
本研究表明,高峰失律内的多灶性发作间期棘波和高幅慢波活动与不同神经网络的激活有关。虽然棘波引起的皮层激活模式与局灶性癫痫相似,但慢波活动在皮层以及脑干、丘脑和壳核等皮层下结构中产生了高峰失律特异性激活。